Canonical Allele Identifier: CA1201822942
Gene: FCER1A HGNC NCBI

Linked Data

dbSNP Id: rs1652080605

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.159288845G>A , CM000663.2:g.159288845G>A GRCh38
NC_000001.10:g.159258635G>A , CM000663.1:g.159258635G>A GRCh37
NC_000001.9:g.157525259G>A NCBI36

Transcript Alleles

HGVS Amino-acid change
NM_002001.3:c.-97-871G>A NP_001992.1:n.-97-871G>A
NM_002001.4:c.-97-871G>A NP_001992.1:n.-97-871G>A